Variant (rsID / SNP)

rs3751631

rs3751631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO5C. Location: chromosome 15, position 52,534,344. The table records no clinical significance for this variant.

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Reference-table entries

MYO5CNot classified

Variant type: synonymous_variant
Chromosome / position: 15:52534344
HGVS: NM_018728.4,c.2457C>T,p.Arg819Arg
Allele change: Synonymous_R819R

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.